Vanlić-Razumenić N, Pujić N, Dedović N, Kostić K, Nastić-Mirić D
Institute of Nuclear Sciences, Vinca, Belgrade, Yugoslavia.
Int J Rad Appl Instrum B. 1992 Apr;19(3):251-6. doi: 10.1016/0883-2897(92)90107-a.
A simplified and efficient procedure for 99mTc-HMPAO-labelling of leukocytes is described. For this purpose, the pH and concentration of the 99mTc-HMPAO preparation was modified. Leukocytes were isolated from a 20 mL mixture of patient blood, 5 mL ACD and 0.8 mL methylcellulose after 1 h sedimentation of erythrocytes and centrifugation (at 400 g) of the obtained plasma layer. Simultaneously, 99mTc-HMPAO was prepared (one single-dose kit for two patients) by adding 2.2 mL 99mTc-generator eluate and, after 10 min, 0.3 mL of phosphate buffer to lower the pH to 7. The isolated WBCs were then labelled by the addition of 1-1.2 mL of 99mTc-HMPAO solution and incubated for 20 min. The unbound tracer was then discarded, the labelled WBC washed and finally resuspended in autologous cell-free plasma. Leukocytes labelled by this procedure were used for scintigraphic localization of inflammatory lesions and abscesses in the gastro-intestinal tract. The labelling efficiency was 60 +/- 9%, with a separation yield of 55 +/- 11%.
描述了一种用于99mTc-HMPAO标记白细胞的简化高效程序。为此,对99mTc-HMPAO制剂的pH值和浓度进行了调整。红细胞沉降1小时后,将患者血液20 mL、ACD 5 mL和甲基纤维素0.8 mL混合,对所得血浆层进行离心(400 g),从中分离白细胞。同时,通过加入2.2 mL 99mTc发生器洗脱液制备99mTc-HMPAO(一个单剂量试剂盒用于两名患者),10分钟后加入0.3 mL磷酸盐缓冲液将pH值降至7。然后加入1 - 1.2 mL 99mTc-HMPAO溶液标记分离出的白细胞,并孵育20分钟。随后弃去未结合的示踪剂,洗涤标记的白细胞,最后重悬于自体无细胞血浆中。通过该程序标记的白细胞用于胃肠道炎症病变和脓肿的闪烁显像定位。标记效率为60±9%,分离产率为55±11%。